MA27075A1 - PHARMACEUTICAL FORMULATIONS FOR THE CONTROLLED RELEASE OF 4-AMINO-6,7-DIMETHOXY-2- (5-METHANESULFONAMIDO-1,2,3,4-TETRAHYDROISOQUINOL-2-YL) -5- (2-PYRIDYL) - QUINAZOLINE - Google Patents

PHARMACEUTICAL FORMULATIONS FOR THE CONTROLLED RELEASE OF 4-AMINO-6,7-DIMETHOXY-2- (5-METHANESULFONAMIDO-1,2,3,4-TETRAHYDROISOQUINOL-2-YL) -5- (2-PYRIDYL) - QUINAZOLINE

Info

Publication number
MA27075A1
MA27075A1 MA27623A MA27623A MA27075A1 MA 27075 A1 MA27075 A1 MA 27075A1 MA 27623 A MA27623 A MA 27623A MA 27623 A MA27623 A MA 27623A MA 27075 A1 MA27075 A1 MA 27075A1
Authority
MA
Morocco
Prior art keywords
tetrahydroisoquinol
quinazoline
dimethoxy
pyridyl
amino
Prior art date
Application number
MA27623A
Other languages
French (fr)
Inventor
Douglas Davis John
James Macrae Ross
John Humphrey Michael
Sarah Smith Janet
Original Assignee
Pfizer
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer filed Critical Pfizer
Publication of MA27075A1 publication Critical patent/MA27075A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0002Galenical forms characterised by the drug release technique; Application systems commanded by energy
    • A61K9/0004Osmotic delivery systems; Sustained release driven by osmosis, thermal energy or gas
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic compounds, e.g. phospholipids, fats
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • A61K9/50Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
    • A61K9/5005Wall or coating material
    • A61K9/5021Organic macromolecular compounds
    • A61K9/5026Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate

Abstract

DEPOSANT Société dite: PFIZER INC. REVENDICATION DE PRIORITES GB 11 Octobre 2001 0124455.7 Voir en annexe le titre de l'invention et le texte de l'abrégé Formulations pharmaceutiques pour la libération contrôlée de la 4-amino-6,7-diméthoxy-2-(5-méthanesulfonamido-1,2,3, 4-tétrahydroisoquinol-2-yl)-5-(2-pyridyl)-quinazoline La présente invention propose une formulation pharmaceutique à libération contrôlée pour administration orale, comprenant de la 4-amino-6,7-diméthoxy-2-(5-méthanesulfonamido-1,2,3,4-tétrahydroisoquinol-2-yl)-5-(2-pyridyl)-quinazoline, ou un de ses sels pharmaceutiquement acceptables, et un adjuvant, diluant ou support pharmaceutiquement acceptable, ladite formulation étant caractérisée en ce qu'elle est adaptée a libérer au moins 50 % en poids de la 4-amino-6,7-diméthoxy-2-(5-méthane-sulfonamido-1,2,3,4-tétrahydroisoquinol-2-yl)-5-(2-pyridyl)-quinazoline, ou de son sel pharmaceutiquement acceptable, au bout de 6 heures dans l'Appareil 1 décrit dans la Pharmacopée des Etats-Unis d'Amérique 24 (2000), pages 1941-1943, comprenant des récipients de 1 litre, des paniers à mailles no. 40 (ouvertures de 0,4 mm), à une vitesse de rotation de 100 tr/min, et avec un milieu de dissolution consistant en 900 ml d'acide chlorhydrique 0,01 M contenant 0,7 % en poids / volume de chlorure de sodium à 37o.C. Les formulations conformes à la présente invention conviennent au traitement de l'hyperplasie prostatique bénigne (HPB).DEPOSITOR Company known as: PFIZER INC. CLAIM OF PRIORITIES GB October 11, 2001 0124455.7 See appendix the title of the invention and the text of the abstract Pharmaceutical formulations for the controlled release of 4-amino-6,7-dimethoxy-2- (5-methanesulfonamido-1 , 2,3,4-tetrahydroisoquinol-2-yl) -5- (2-pyridyl) -quinazoline The present invention provides a controlled release pharmaceutical formulation for oral administration comprising 4-amino-6,7-dimethoxy- 2- (5-methanesulfonamido-1,2,3,4-tetrahydroisoquinol-2-yl) -5- (2-pyridyl) -quinazoline, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable adjuvant, diluent or carrier, said formulation being characterized in that it is adapted to release at least 50% by weight of 4-amino-6,7-dimethoxy-2- (5-methane-sulfonamido-1,2,3,4-tetrahydroisoquinol- 2-yl) -5- (2-pyridyl) -quinazoline, or its pharmaceutically acceptable salt, after 6 hours in Device 1 described in the United States Pharmacopoeia is of America 24 (2000), pages 1941-1943, including 1 liter containers, mesh baskets no. 40 (0.4 mm openings), at a rotational speed of 100 rpm, and with a dissolution medium consisting of 900 ml of 0.01 M hydrochloric acid containing 0.7% w / v chloride sodium at 37o C. The formulations according to the present invention are suitable for the treatment of benign prostatic hyperplasia (HPB).

MA27623A 2001-10-11 2004-04-08 PHARMACEUTICAL FORMULATIONS FOR THE CONTROLLED RELEASE OF 4-AMINO-6,7-DIMETHOXY-2- (5-METHANESULFONAMIDO-1,2,3,4-TETRAHYDROISOQUINOL-2-YL) -5- (2-PYRIDYL) - QUINAZOLINE MA27075A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0124455.7A GB0124455D0 (en) 2001-10-11 2001-10-11 Pharmaceutical formulations

Publications (1)

Publication Number Publication Date
MA27075A1 true MA27075A1 (en) 2004-12-20

Family

ID=9923660

Family Applications (1)

Application Number Title Priority Date Filing Date
MA27623A MA27075A1 (en) 2001-10-11 2004-04-08 PHARMACEUTICAL FORMULATIONS FOR THE CONTROLLED RELEASE OF 4-AMINO-6,7-DIMETHOXY-2- (5-METHANESULFONAMIDO-1,2,3,4-TETRAHYDROISOQUINOL-2-YL) -5- (2-PYRIDYL) - QUINAZOLINE

Country Status (32)

Country Link
EP (1) EP1434570B8 (en)
JP (1) JP4131471B2 (en)
KR (1) KR20050032510A (en)
CN (1) CN1568180A (en)
AP (1) AP2004003001A0 (en)
AR (1) AR036782A1 (en)
AT (1) ATE303135T1 (en)
BR (1) BR0213196A (en)
CA (1) CA2461168A1 (en)
CO (1) CO5560534A2 (en)
DE (1) DE60205925T2 (en)
DK (1) DK1434570T3 (en)
DO (1) DOP2002000464A (en)
EA (1) EA006168B1 (en)
ES (1) ES2246017T3 (en)
GB (1) GB0124455D0 (en)
GT (1) GT200200184A (en)
HR (1) HRP20040261A2 (en)
HU (1) HUP0600064A3 (en)
IL (1) IL160969A0 (en)
IS (1) IS7179A (en)
MA (1) MA27075A1 (en)
MX (1) MXPA04003293A (en)
NO (1) NO20041520L (en)
OA (1) OA12709A (en)
PA (1) PA8556001A1 (en)
PE (1) PE20030551A1 (en)
PL (1) PL369666A1 (en)
SV (1) SV2004001279A (en)
UY (1) UY27477A1 (en)
WO (1) WO2003032956A1 (en)
ZA (1) ZA200401976B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0317663D0 (en) * 2003-07-29 2003-09-03 Astrazeneca Ab Pharmaceutical composition
HUE052355T2 (en) 2013-03-14 2021-04-28 Amgen Inc Heterocyclic compounds and their uses
KR101943592B1 (en) 2017-08-31 2019-01-30 조현우 Electronic Household Accounting System using Data Mining Techniques

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2053120T3 (en) * 1990-07-02 1994-07-16 Bend Res Inc ASYMMETRIC MICROPOROUS PEARLS FOR CONTROLLED RELEASE.
FR2752737B1 (en) * 1996-08-29 1998-10-02 Synthelabo CONTROLLED RELEASE TABLET OF ALFUZOSINE HYDROCHLORIDE
GB9700504D0 (en) * 1997-01-11 1997-02-26 Pfizer Ltd Pharmaceutical compounds
IL141235A (en) * 2000-02-09 2012-04-30 Novartis Int Pharm Ltd Combined use of an alpha-adrenoceptor antagonist and a muscarinic antagonist in the manufacture of a medicament for the treatment of benign prostatic hyperplasia
SK12282002A3 (en) * 2000-03-03 2003-10-07 Pfizer Inc. 4-Amino-6,7-dimethoxy-2-(5-methanesulfonamido-1,2,3,4- tetrahydroisoquinol-2-yl)-5-(2-pyridyl)quinazoline mesylat and polymorphs

Also Published As

Publication number Publication date
PE20030551A1 (en) 2003-06-26
EP1434570B1 (en) 2005-08-31
HUP0600064A3 (en) 2007-02-28
GT200200184A (en) 2003-05-23
OA12709A (en) 2006-06-26
GB0124455D0 (en) 2001-12-05
IL160969A0 (en) 2004-08-31
EA006168B1 (en) 2005-10-27
HRP20040261A2 (en) 2004-08-31
WO2003032956A1 (en) 2003-04-24
JP2005507909A (en) 2005-03-24
IS7179A (en) 2004-03-11
EP1434570A1 (en) 2004-07-07
HUP0600064A2 (en) 2006-06-28
MXPA04003293A (en) 2004-07-23
PA8556001A1 (en) 2003-07-28
DOP2002000464A (en) 2003-04-15
CO5560534A2 (en) 2005-09-30
DK1434570T3 (en) 2005-11-07
AP2004003001A0 (en) 2004-03-31
KR20050032510A (en) 2005-04-07
EP1434570B8 (en) 2005-10-26
UY27477A1 (en) 2003-05-30
SV2004001279A (en) 2004-02-19
ZA200401976B (en) 2004-07-12
NO20041520L (en) 2004-04-05
JP4131471B2 (en) 2008-08-13
EA200400431A1 (en) 2004-08-26
AR036782A1 (en) 2004-10-06
PL369666A1 (en) 2005-05-02
DE60205925T2 (en) 2006-06-08
ES2246017T3 (en) 2006-02-01
CA2461168A1 (en) 2003-04-24
DE60205925D1 (en) 2005-10-06
BR0213196A (en) 2004-08-31
ATE303135T1 (en) 2005-09-15
CN1568180A (en) 2005-01-19

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